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Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

Sfrp2 increases during hair follicle catagen phase and slows keratinocyte growth.

Scube3 gene affects mouse embryo growth in multiple areas, but needs more research.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

The study found potential new DNA patterns in fertility genes, but further testing is needed.

Gremlin proteins help regulate hair growth by balancing signals in hair follicles.

The Siah1 and Siah2 genes are active in mouse skin development and hair growth, especially right after birth.

Certain variations of the HDAC9 gene can increase or decrease stroke risk in the Chinese population.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Defective protein folding due to a mutation is key in ANE syndrome.

PrrH sRNA controls pyochelin gene expression in Pseudomonas aeruginosa based on heme levels.

The hairless gene is crucial for hair health, and its mutations cause hair loss.

Certain genes controlled by OVOL1 are crucial for creating new hair follicles.

Overexpression of sPLA2-IIA in mouse skin reduces hair stem cells and increases cell differentiation through JNK/c-Jun pathway activation.

The research identified specific genes that are active in the cells crucial for hair growth.

The research found changes in gene expression related to cell death in mouse skin that help understand hair follicle development and skin health.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Wnt genes help starfish regrow arms by aiding wound healing and cell development.

The TGM3 gene's promoter region is key for skin and hair cell function and may aid gene therapy.

The FOS gene helps hair growth in Tan sheep.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

ILC1-like cells can cause alopecia areata by themselves.

Mutations in the P2RY5 gene cause hereditary woolly hair.

Meis1 is crucial for skin health and tumor development.

Targeting the TNFRSF1B gene may help treat hair loss.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

The scraggly mutation causes hair loss and skin defects in mice.